HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 4-Hydroxy-2,3,6-trimethylphenyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trimethylhydroquinone | HCID 12785 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Hydroxy-2,3,6-trimethylphenyl acetate | HCID 119024 | — |
Reaction Steps
Stir a mixture of trimethylhydroquinone (15.2 g, 0.1 mol), triethylamine (25.3 g, 0.25 mol) and ether (500 mL) in an ice bath. Slowly add acetylchloride (19.6 g, 0.25 mol) with stirring, allow the reaction to warm to room temperature for an hour, then dilute with water and the separate the layers. Evaporate the ether layer to dryness. Dissolve the resulting diacetate in methanol (300 mL). Add strong ammonium hydroxide (11 mL) and stir the mixture at room temperature overnight. Distill off the solvents under reduced pressure and dissolve the residue in ether. Wash the ether layer with water and evaporate to dryness. Recrystallization from hexane-ether yields 4-acetoxy-2,3,5-trimethylphenol (16.7 g, m.p.=106-107° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06114572 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-4e451afb1bf44ce0b6eb856113310da6 |
| Source note | uspto-grants-2000_09 |